Van Ameringen M A, Lane R M, Walker J R, Bowen R C, Chokka P R, Goldner E M, Johnston D G, Lavallee Y J, Nandy S, Pecknold J C, Hadrava V, Swinson R P
Anxiety Disorders Clinic, McMaster University Medical Centre, Hamilton, Canada.
Am J Psychiatry. 2001 Feb;158(2):275-81. doi: 10.1176/appi.ajp.158.2.275.
The authors evaluated the efficacy, safety, and tolerability of sertraline, a selective serotonin reuptake inhibitor, in the treatment of generalized social phobia.
Adult outpatients with generalized social phobia (N=204) from 10 Canadian centers were randomly assigned to receive sertraline or placebo in a 2:1 ratio for a 20-week double-blind study following a 1-week, single-blind, placebo run-in. The initial dose of sertraline was 50 mg/day with increases of 50 mg/day every 3 weeks permitted after the fourth week of treatment (dosing was flexible up to a maximum of 200 mg/day). Primary efficacy assessments were the percentage of patients rated much or very much improved on the Clinical Global Impression (CGI) improvement item and the mean changes from baseline to study endpoint in total score on the social phobia subscale of the Marks Fear Questionnaire and total score on the Brief Social Phobia Scale.
In intent-to-treat endpoint analyses of 203 of the patients, significantly more of the 134 patients given sertraline (N=71 [53%]) than of the 69 patients receiving placebo (N=20 [29%]) were considered responders according to their CGI improvement scores at the end of treatment. The mean reductions in the social phobia subscale of the Marks Fear Questionnaire and in the total score on the Brief Social Phobia Scale were 32.6% and 34.3% in the sertraline group and 10.8% and 18.6% in the placebo group, respectively. Analysis of covariance showed superiority of sertraline over placebo on all primary and secondary efficacy measures. Sertraline was well tolerated: 103 (76%) of the 135 sertraline-treated patients and 54 (78%) of the 69 placebo-treated patients completed the study.
Sertraline is an effective treatment for patients with generalized social phobia.
作者评估了选择性5-羟色胺再摄取抑制剂舍曲林治疗广泛性社交恐惧症的疗效、安全性及耐受性。
来自加拿大10个中心的204例成年广泛性社交恐惧症门诊患者,在为期1周的单盲安慰剂导入期后,以2:1的比例随机分配接受舍曲林或安慰剂治疗,进行为期20周的双盲研究。舍曲林初始剂量为50mg/天,治疗第4周后每3周可增加50mg/天(剂量灵活调整,最大剂量为200mg/天)。主要疗效评估指标为在临床总体印象量表(CGI)改善项目中评定为显著或非常显著改善的患者百分比,以及从基线到研究终点,马克斯恐惧问卷社交恐惧症分量表总分和简易社交恐惧症量表总分的平均变化。
在对203例患者的意向性治疗终点分析中,根据治疗结束时的CGI改善评分,接受舍曲林治疗的134例患者中有71例(53%)被视为有效者,显著多于接受安慰剂治疗的69例患者中的20例(29%)。舍曲林组马克斯恐惧问卷社交恐惧症分量表总分及简易社交恐惧症量表总分的平均降幅分别为32.6%和34.3%,安慰剂组分别为10.8%和18.6%。协方差分析显示,在所有主要和次要疗效指标上舍曲林均优于安慰剂。舍曲林耐受性良好:135例接受舍曲林治疗的患者中有103例(76%)、69例接受安慰剂治疗的患者中有54例(78%)完成了研究。
舍曲林是治疗广泛性社交恐惧症患者的有效药物。